Order Article Reprints

Hassoun R, Budde H, Mannherz HG, Lódi M, Fujita-Becker S, Laser KT, Gärtner A, Klingel K, Möhner D, Stehle R, et al. De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents. International Journal of Molecular Sciences. 2021; 22(17):9625. https://doi.org/10.3390/ijms22179625

Hassoun, Roua, Heidi Budde, Hans Georg Mannherz, Mária Lódi, Setsuko Fujita-Becker, Kai Thorsten Laser, Anna Gärtner, Karin Klingel, Desirée Möhner, Robert Stehle, and et al. 2021. "De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents" International Journal of Molecular Sciences 22, no. 17: 9625. https://doi.org/10.3390/ijms22179625

Hassoun, R., Budde, H., Mannherz, H. G., Lódi, M., Fujita-Becker, S., Laser, K. T., Gärtner, A., Klingel, K., Möhner, D., Stehle, R., Sultana, I., Schaaf, T., Majchrzak, M., Krause, V., Herrmann, C., Nowaczyk, M. M., Mügge, A., Pfitzer, G., Schröder, R. R., ... Cimiotti, D. (2021). De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents. International Journal of Molecular Sciences, 22(17), 9625. https://doi.org/10.3390/ijms22179625